Browsing by Author "Jeon, D. W."

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    Efficient nonradiative energy transfer from InGaN/GaN nanopillars to CdSe/ZnS core/shell nanocrystals
    (AIP Publishing, 2011-04-20) Nizamoglu, S.; Guzelturk, B.; Jeon, D. W.; Lee, I. H.; Demir, Hilmi Volkan
    In this study, we propose and demonstrate efficient electron-hole pair injection from InGaN/GaN multiple quantum well nanopillars (MQW-NPs) to CdSe/ZnS core/shell nanocrystal quantum dots (NQDs) via Forster-type nonradiative energy transfer. For that we hybridize blue-emitting MQW-NPs with red-emitting NQDs and the resultant exciton transfer reaches a maximum rate of (0.192 ns)(-1) and a maximum efficiency of 83.0%. By varying the effective bandgap of core/shell NQDs, we conveniently control and tune the excitonic energy transfer rate for these NQD integrated hybrids, and our measured and computed exciton transfer rates are found to be in good agreement for all hybrid cases.
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    Morphology-dependent energy transfer of polyfluorene nanoparticles decorating InGaN/GaN quantum-well nanopillars
    (American Chemical Society, 2013) Erdem, T.; Ibrahimova, V.; Jeon, D. W.; Lee, I. H.; Tuncel, D.; Demir, Hilmi Volkan
    Conjugated polymer nanoparticles (CPNs), prepared in aqueous dispersion from poly[(9,9-bis{3- bromopropyl}fluorenyl-2,7-diyl)-co-(1,4-benzo-{2,1,3}-thiodiazole)] (PFBT-Br), are incorporated into a nanopillar architecture of InGaN/GaN multiple quantum wells (MQWs) to demonstrate a new organic/inorganic class of nanostructured excitonic model system. This hybrid system enables intimate integration for strong exciton−exciton interactions through nonradiative energy transfer (NRET) between the integrated CPNs and MQW pillars. The NRET of these excitonic systems is systematically investigated at varied temperatures. In these hybrids, InGaN/GaN MQWs serve as the donor of the NRET pair, while immobilized PFBT-Br polymer serves as the acceptor. To understand morphology-dependent NRET, PFBT-Br CPNs coating InGaN/GaN MQWs are made to defold into polymer chains by in situ treatment with a good solvent (THF). The experimental results indicate that NRET is significantly stronger in the case of CPNs compared with their defolded polymer chains. At room temperature, while the NRET efficiency of open polymer chains−nanopillar system is only 10%, PFBT-Br CPNs exhibit a substantially higher NRET efficiency of 33% (preserving the total number of polymer molecules). The NRET efficiency of the nanoparticle systems is observed to be 25% at 250 K, 22% at 200 K, 19% at 150 K, and 15% at 100 K. On the other hand, the defolded polymer chains exhibit significantly lower NRET efficiencies of 17% at 250 K, 16% at 200 K, 11% at 150 K, and 5% at 100 K. This work may potentially open up new opportunities for the hybrid organic/inorganic systems where strong excitonic interactions are desired for light generation, light harvesting, and sensing applications.